Acoustic transmission enhancement through a periodically-structured stiff plate without any opening

We report both experimentally and theoretically that the enhanced acoustic transmission can occur in the subwavelength region through a thin but stiff structured-plate without any opening. This exotic acoustic phenomenon is essentially distinct from the previous related studies originated from, either collectively or individually, the interaction of the incident wave with openings in previous structures. It is attributed to the structure-induced resonant excitation of the non-leaky Lamb modes that exist intrinsically in the uniform elastic plate. Our finding should have impact on ultrasonic applications.Comment: 11 pages, 4 figure

Evidence for potential and inductive convection during intense geomagnetic events using normalized superposed epoch analysis

The relative contribution of storm‐time ring current development by convection driven by either potential or inductive electric fields has remained an unresolved question in geospace research. Studies have been published supporting each side of this debate, including views that ring current buildup is entirely one or the other. This study presents new insights into the relative roles of these storm main phase processes. We perform a superposed epoch study of 97 intense ( Dst Min    Dst Min  > –100 nT) storms using OMNI solar wind and ground‐based data. Instead of using a single reference time for the superpositioning of the events, we choose four reference times and expand or contract each phase of every event to the average length of this phase, creating a normalized timeline for the superposed epoch analysis. Using the bootstrap method, we statistically demonstrate that timeline normalization results in better reproduction of average storm dynamics than conventional methods. Examination of the Dst reveals an inflection point in the intense storm group consistent with two‐step main phase development, which is supported by results for the southward interplanetary magnetic field and various ground‐based magnetic indices. This two‐step main‐phase process is not seen in the moderate storm timeline and data sets. It is determined that the first step of Dst development is due to potential convective drift, during which an initial ring current is formed. The negative feedback of this hot ion population begins to limit further ring current growth. The second step of the main phase, however, is found to be a more even mix of potential and inductive convection. It is hypothesized that this is necessary to achieve intense storm Dst levels because the substorm dipolarizations are effective at breaking through the negative feedback barrier of the existing inner magnetospheric hot ion pressure peak. Key Points Moderate and intense geomagnetic storms Evidence for potential and inductive convection Normalized superposed epoch analysisPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/97285/1/jgra50014.pd

The inner centromere is a biomolecular condensate scaffolded by the chromosomal passenger complex.

The inner centromere is a region on every mitotic chromosome that enables specific biochemical reactions that underlie properties, such as the maintenance of cohesion, the regulation of kinetochores and the assembly of specialized chromatin, that can resist microtubule pulling forces. The chromosomal passenger complex (CPC) is abundantly localized to the inner centromeres and it is unclear whether it is involved in non-kinase activities that contribute to the generation of these unique chromatin properties. We find that the borealin subunit of the CPC drives phase separation of the CPC in vitro at concentrations that are below those found on the inner centromere. We also provide strong evidence that the CPC exists in a phase-separated state at the inner centromere. CPC phase separation is required for its inner-centromere localization and function during mitosis. We suggest that the CPC combines phase separation, kinase and histone code-reading activities to enable the formation of a chromatin body with unique biochemical activities at the inner centromere

Imaging Chromophores With Undetectable Fluorescence by Stimulated Emission Microscopy

Fluorescence, that is, spontaneous emission, is generally more sensitive than absorption measurement, and is widely used in optical imaging. However, many chromophores, such as haemoglobin and cytochromes, absorb but have undetectable fluorescence because the spontaneous emission is dominated by their fast non-radiative decay. Yet the detection of their absorption is difficult under a microscope. Here we use stimulated emission, which competes effectively with the nonradiative decay, to make the chromophores detectable, and report a new contrast mechanism for optical microscopy. In a pump-probe experiment, on photoexcitation by a pump pulse, the sample is stimulated down to the ground state by a time-delayed probe pulse, the intensity of which is concurrently increased. We extract the miniscule intensity increase with shot-noise-limited sensitivity by using a lock-in amplifier and intensity modulation of the pump beam at a high megahertz frequency. The signal is generated only at the laser foci owing to the nonlinear dependence on the input intensities, providing intrinsic three-dimensional optical sectioning capability. In contrast, conventional one-beam absorption measurement exhibits low sensitivity, lack of three-dimensional sectioning capability, and complication by linear scattering of heterogeneous samples. We demonstrate a variety of applications of stimulated emission microscopy, such as visualizing chromoproteins, non-fluorescent variants of the green fluorescent protein, monitoring lacZ gene expression with a chromogenic reporter, mapping transdermal drug distributions without histological sectioning, and label-free microvascular imaging based on endogenous contrast of haemoglobin. For all these applications, sensitivity is orders of magnitude higher than for spontaneous emission or absorption contrast, permitting nonfluorescent reporters for molecular imaging.Chemistry and Chemical Biolog